# FDA recall Z-0401-2022

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2021-12-03.

## Product

Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x 18mm, a component of the CHARLOTTE Lisfranc Reconstruction System.

## Reason for recall

Incorrect product is contained in the packaging.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, IA, and SC.  The countries of Australia, Canada, Chile, Spain, and United Kingdom.

## Key facts

- **Recall number:** Z-0401-2022
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-12-03
- **Report date:** 2021-12-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0401-2022

## Citation

> AI Analytics. FDA recall Z-0401-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0401-2022. Source: US FDA. Licensed CC0.

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